Paper Strips Research Articles

Comment on “Cellular aggregation dictates universal spreading behaviour of a whole-blood drop on a paper strip”

Laha et al. studied the diffusive behavior of a whole-blood drop on filter paper using the generalized capillary bundle model. However, some model parameters should be further refined to accurately reflect the physics involved in this diffusion process. Moreover, citations are missing for some key equations. Addressing these aspects will improve the model applicability to this application and benefit readers in accessing more accurate and detailed information.

An eugenol-sulfonyl based fluorescent probe for recognition of Al3+ in real sample analysis and biological application

The present work describes an eugenol-sulfonyl based fluorescence chemosensor, H4L [H4L=6,6′-((1E,1′E)-((sulfonylbis(6-hydroxy-3,1- phenylene))bis(azanylylidene))bis(methanylylidene))bis(4-allyl-2-methoxyphenol)], which shows maximum emission intensity towards Al3+ ion in presence of other competing metal ions. Upon excitation at 440 nm H4L exhibits a significant rise in fluorescence at 547 nm upon gradual addition of Al3+ ion in the HEPES buffer at pH=7.4 (MeOH:H2O, 4:1, (v/v)). The increasing value of fluorescence is mainly due to chelation enhanced fluorescence effect (CHEF). Complete characterization of the probe (H4L) and metal bound complex (1) have been determined using a range of methods including UV–Vis absorption titration, fluorescence titration, NMR, ESI-mass, etc. Thus 1:2 binding stoichiometry between H4L and metal ion has been also proved. Another important aspect: regeneration and reversibility of H4L are investigated in presence of Na2EDTA. H4L exhibits ∼ 10−6 M order detection limit and significant binding constant (∼106 M−1) for the Al3+ ion, suggesting its potential use in bio-imaging studies. The probe was effectively used in real samples as well as paper strip to locate the Al3+ ion.

An all-in-one smartphone-assisted ratiometric fluorescent device for visual and quantitative detection of glutathione

The daily consumption of foods abundant in Glutathione (GSH) can be supplemented to maintain the homeostasis of GSH in human health and alleviate pathologies resulting from abnormal GSH levels. The fluorescence-based visual determination of GSH has gradually attracted the attention of researchers due to its robust performance and versatile implementation. However, the current GSH visual strategy primarily relies on variations in fluorescence intensity at a single emission wavelength, which poses challenges for naked-eye and portable readout, as well as distorted signals caused by complex matrix effects in real samples. Herein, a ratiometric fluorescence sensor based on carbon dots (CDs) combined with an all-in-one 3D-printed smartphone-based device was successfully developed for low-cost, visual and rapid detection of GSH without the need for an external excitation light source. The ratiometric fluorescent materials were synthesized by conjugating blue carbon dots (B-CDs) with yellow carbon dots (Y-CDs) through the utilization of selected Cu2+ ions. The resulting mechanism demonstrated that the coordination interaction between Cu2+ and residual aromatic amino groups in Y-CDs (Y-CDs-Cu2+) contributed to a newly emitted peak at 580 nm, thereby inducing fluorescence resonance energy transfer from B-CDs to Y-CDs-Cu2+. A linear correlation was found between GSH concentrations and R/B values in the range of 10–100 μM, with a limit of detection observed at 4.8 μM. By utilizing this portable device in combination with RGB analysis, the quantitative detection of GSH can be achieved even in complex food matrices such as tomatoes and grapes. The universality of this all-in-one device was further validated by pre-spraying CDs onto a paper strip for visual measurement of GSH. This work offers a portable, visual, and accessible approach to evaluating food safety and nutrition, thereby demonstrating significant economic value and holding profound implications for human health.

A microfluidic paper-based fluorescent sensor integrated with a smartphone platform for rapid on-site detection of omethoate pesticide

A novel approach combing a fluorescent microfluidic paper strip with a portable smartphone-based sensing platform is developed for rapid and sensitive detection of omethoate pesticide. The detection mechanism of the microfluidic paper strip is based on the fluorescence quenching of graphene oxide (GO) toward the cyanine 3 (Cy3)-labeled aptamer (Cy3-APT). Upon exposure to omethoate, the Cy3-APT detaches from the surface of GO, resulting in considerable fluorescence recovery, which can be visualized through the smartphone-based sensing platform. The images are analyzed through a self-developed app embedded with a pretrained convolutional neural network model, achieving a high regression coefficient of 0.9964 at an omethoate concentration range of 0–750 nM. The smartphone-based platform enables rapid on-site detection of omethoate pesticide in real samples within 10 min, with results comparable to those obtained using standard methods. In short, the proposed microfluidic paper-based fluorescent sensor combined with the smartphone-based sensing platform enhances the detection performance toward organophosphorus pesticides.

Chromogenic Chemosensor for Simultaneous Detection of PO4 3- and CO3 2- Anions in Organo-Aqueous Solutions: Application in Arduino Based Electronic Color Sensor Device and Logic Gate.

Three new chromogenic receptors have been synthesized with the primary objective of facilitating the selective recognition of PO4 3-and CO3 2- ions in an organo-aqueous medium. R1 and R2 exhibit an extraordinary detection limit aligning with both EPA and WHO guidelines. R1 shows LOD of 0.135 ppm for PO4 3- and 0.175 ppm for CO3 2-, while R2 sets forth a LOD of 0.427 ppm for PO4 3- and 0.729 ppm for CO3 2-. The binding mechanism involves intramolecular charge transfer (ICT) band are substantiated by comprehensive studies that include UV-Vis titration, 1H-NMR titration, DFT studies and electrochemical studies. Chemosensors were employed in the formulation of logic gate, the fabrication of a paper strip test kit and its application in RGB color sensor device.

Synthesis of Multifunctional Chemosensors for Naked Eye Detection of Cu2+ and Hg2+; Application in Paper Strips, Water, and Food Sample

AbstractThree chemosensors ISA‐1, ISA‐2, and ISA‐3 were synthesized for the detection of Cu2+ and Hg2+ ions in a 50% H₂O‐DMF solution. ISA‐1 is specifically designed for the detection of Cu2+ ions, while ISA‐2 can detect both Cu2⁺ and Hg2⁺ ions. Upon interaction with Cu2⁺, ISA‐1 undergoes a naked‐eye colorimetric transition from pink to blue. ISA‐2 exhibits a similar pink‐to‐blue color change in the presence of Cu2+ ion, however, colorless when exposed to Hg2+ ion. The detection limits for Cu2+ using ISA‐1 and ISA‐2 are 0.574 ppm and 0.0074 ppm, respectively, both of which are significantly lower than the WHO guideline of ≤1.5 ppm for Cu2+ in drinking water. These chemosensors have also been successfully integrated into paper strips and logic gate systems and applied for the analysis of water and food samples.

Green synthesis of carbon dots from Hakka yellow wine lees: Characterization and applications for Fe3+ and NaFeEDTA sensing

In this study, Hakka yellow wine lees carbon dots (HYWL-CDs) with an average diameter of 1.75 nm are synthesized from Hakka yellow wine lees (HYWL) via a one-pot hydrothermal method. Results of X-ray photoelectron spectroscopy and FTIR reveal the presence of C=C and –OH in the HYWL-CDs. Additionally, the HYWL-CDs present excitation-wavelength dependence, with maximum excitation and emission wavelengths of 360 and 440 nm, respectively. The fluorescence of the HYWL-CDs can be quenched by Fe3+. The Fe3+ concentration is correlated linearly with the quenching rate over a linear range of 0.6–1.1 mg/mL, and the limit of detection is 0.18 μg/mL. And phenols have been shown to be present in HYWL-CDs, and the color reaction between phenols and FeCl3 is most likely the mechanism by which FeCl3 causes fluorescence burst in HYWL-CDs. Moreover, the HYWL-CDs demonstrate significant potential for detecting NaFeEDTA in iron-fortified soy sauces, the linear-fit equation was y = 185.38x + 1024.6 (R2 = 0.9995) The HYWL-CDs are loaded onto paper strips, iron-fortified straw mushroom dark soy sauce showed noticeable color changes, which allows one to differentiate normal soy sauce from iron-fortified soy sauce more conveniently and provides a new perspective for the high-value utilization of yellow wine lees.

Pyrazole appended Schiff base based sensor for Al3+ detection: Spectroscopic investigation, real sample analysis and cell imaging studies

Herein, we are reporting a new pyrazole derived chemosensor named H2QPC [(E)-N’-((2-hydroxyquinolin-3-yl)methylene)-3-methyl-1H-pyrazole-5-carbohydrazide] exhibiting selective “off–on” fluorimetric response towards Al3+ ion in different solvents. The probe exhibited a submicromolar detection level (LOD = 0.37 μM) for the Al3+. The density functional theory (DFT) and time dependent DFT (TD-DFT) of the probe and corresponding Al3+-complex revealed that a change of structural conformation of probe H2QPC upon complexation. The pyrazole unit creates a specific cavity to tether Al3+, and consequently H2QPC shows as a promising molecule for Al3+ detection. Further, the probe has been used successfully for qualitative determination of Al3+ using filter paper strips. The in situ Al3+ ion cell imaging in HCT116 cells discloses the cellular penetrability of the sensor, and holds pronounced promise for application in biological and environment sciences.

Insecticidal and Repellent Activity of Essential Oils from Copaifera reticulata, Citrus paradisi, Lavandula hybrida and Salvia sclarea Against Immature and Adult Stages of Ctenocephalides felis felis.

The flea Ctenocephalides felis (Siphonaptera: Pulicidae), parasitizes dogs and cats globally, acting as a vector for various pathogens affecting both animals and humans. Growing interest in environmentally friendly, plant-based products prompted this study. The aim of the study was to determine the chemical composition of essential oils (EOs) from Copaifera reticulata, Citrus paradisi, Lavandula hybrida and Salvia sclarea, assessing their insecticidal and repellent properties, determining lethal concentrations (LC50 and LC90), and evaluating residual efficacy in vitro against Ctenocephalides felis felis. Gas Chromatography with Flame Ionization Detector analyzed EO composition. In vitro tests involved preparing EO solutions at various concentrations. Ten specimens from each life stage (egg, larva, pupa, adult) were used for insecticidal activity assessment. Adulticidal activity was assessed using 10cm2 filter paper strip, each treated with 0.200mL of the test solution. Immature stages activities were evaluated using 23.76cm2 discs of the same filter paper, each treated with 0.470mL of the test solution. Mortality percentage was calculated using (number of dead insects × 100) / number of incubated insects. Probit analysis calculated LC50 values with a 95% confidence interval. Major EO constituents were β-caryophyllene (EOCR), linalool (EOLH), linalyl acetate (EOSS), and limonene (EOCP). LC50 values were obtained for all stages except for the essential oil of C. paradisi. All oils showed repellent activity at 800μg/cm2. OECR exhibited greater residual efficacy. Each EO demonstrated superior insecticidal activity against specific C. felis felis stages.

Detecting dissolved mercury(ii) ions using chitosan-AgNP strips integrated with smartphones.

A simple preparation of a paper strip test with a smartphone-based instrument for detecting dissolved mercury is still in development. This study aims to develop a smartphone-based colorimetric paper strip test using chitosan-stabilized silver nanoparticles for detecting dissolved mercury. The method demonstrated high sensitivity and selectivity for Hg2+ ions, with detection limits comparable to UV-vis spectrophotometry. Silver ions embedded in the chitosan matrix were reduced by either sodium NaBH4 or N2H4. Both chi-AgNP colloidal and chi-AgNP paper strips were tested for sensitivity of mercury(ii) solution detection with and without ion interference. The accuracy of colour change responding to the mercury concentration was recorded with several smartphones in a handmade cubical and a T-shape micro-studio. Only NaBH4 gives colloidal chi-AgNPs relatively dispersed, and the colloidal chi-AgNPs become aggregated when AgNP interacts with mercury(ii) ions. The colour change of chi-AgNP paper strips responding to the concentration of mercury(ii) and quantified using a smartphone is consistent when confirmed with UV-vis spectrophotometric determination with a comparable limit of detection (0.76 μM). The inferring ions do not significantly affect mercury(ii) analyses. Therefore, the paper strip integrated with the smartphone is effectively used for mercury(ii) detection in water as long as the mercury concentration is >1 μM. This finding might inspire advanced technology with a larger number of data references, and machine learning involvement to develop more compatible and simple mercury detection.

Red-emitting copper nanoclusters for ultrasensitive and selective detection of creatinine and its application in portable smartphone-based paper strips and polymer thin film

In this work, a quantitative paper-based sensor integrated with smartphone-application was developed using poly(sodium 4-styrenesulfonate) stabilized copper nanoclusters (PSS-CuNCs) as a fluorescence probe to detect creatinine (CRN). The surface morphology and optical properties of PSS-CuNCs were verified using UV–vis absorption, zeta-potential, photoluminescence, high resolution transmission electron microscopy (HR-TEM) and Fourier-transform infrared (FI-IR) and X-ray photoelectron (XPS) spectroscopy. PSS-CuNCs exhibited strong red fluorescence with the emission peak centered at 654 nm upon excitation at 390 nm. PSS-CuNCs was also used to determine CRN because of their excellent fluorescence properties. The fluorescence of PSS-CuNCs was quenched significantly by adding different concentrations of CRN, which mainly originated from the formation of ground state complexation. The PSS-CuNCs probe showed high sensitivity with a low limit of detection (LOD) of 2.48 nM and high selectivity even in the presence of other interfering analytes. This assay was also used to measure CRN in real samples. Additionally, test paper-based assay has been developed to detect CRN using smartphones. The developed assay provides a reliable, cost-effective, sensitive and portable on-site method to measure CRN levels by utilizing fluorescence color changes. Incorporation of PSS-CuNCs into poly(vinyl alcohol) resulted in the formation of fluorescent transparent polymer thin films with high photostability.

Establishment of a Rapid Detection Method for Cadmium Ions via a Specific Cadmium Chelator N-(2-Acetamido)-Iminodiacetic Acid Screened by a Novel Biological Method.

Heavy metal ions such as cadmium, mercury, lead, and arsenic in the soil cannot be degraded naturally and are absorbed by crops, leading to accumulation in agricultural products, which poses a serious threat to human health. Therefore, establishing a rapid and efficient method for detecting heavy metal ions in agricultural products is of great significance to ensuring the health and safety. In this study, a novel optimized spectrometric method was developed for the rapid and specific colorimetric detection of cadmium ions based on N-(2-Acetamido)-iminodiacetic acid (ADA) and Victoria blue B (VBB) as the chromogenic unit. The safety evaluation of ADA showed extremely low biological toxicity in cultured cells and live animals. The standard curve is y = 0.0212x + 0.1723, R2 = 0.9978, and LOD = 0.08 μM (0.018 mg/kg). The liner concentrations detection range of cadmium is 0.1-10 μM. An inexpensive paper strip detection method was developed with a detection limit of 0.2 μM to the naked eye and a detection time of less than 1 min. The method was successfully used to assess the cadmium content of rice, soybean, milk, grape, peach, and cabbage, and the results correlated well with those determined by inductively coupled plasma-mass spectrometry (ICP-MS). Thus, our study demonstrated a novel rapid, safe, and economical method for onsite, real-time detection of cadmium ions in agricultural products.

Enhanced pyrophosphate detection: Utilizing oPD-derived carbon dots and Fe3+ interactions in a paper strip biosensor

The development of portable, cost-effective, and straightforward DNA biosensors holds immense importance in various fields, including healthcare, environmental monitoring, and food safety. This study contributes to the objective by introducing an innovative approach for synthesizing carbon dots (Cdots) with high quantum yield (QY) and remarkable selectivity for Fe3+ ions. Utilizing o-phenylenediamine as a precursor, the study achieved a straightforward and environmentally friendly synthesis method, enabling the efficient detachment of metal ions from the Cdot surface upon introducing pyrophosphate (PPi). The presence of surface hydroxyl and amino groups facilitated specific Fe3+ recognition. Employing D-optimal response surface methodology, the study optimized Cdot synthesis parameters, identifying temperature and heating time as critical factors influencing QY. Statistical analysis confirmed the model's reliability, predicting maximum QY of 48.8 % with minimal deviation from experimental results. Characterization studies revealed the amorphous nature of Cdots through HR-TEM, XRD, and FTIR analysis. Furthermore, the proposed LAMP/PPi biosensing technique demonstrated higher sensitivity, specificity, and repeatability, with negligible interference from common anions and efficacy across varying pH levels. The limit of detection (LOD) of 0.079 (±0.01) μM and the detection range of 0.1 μM–2 mM underscore the biosensor's practical utility. This study highlights a promising direction for developing paper-based LAMP/PPi biosensors with potential diagnostics and environmental monitoring applications. Significantly, the biosensing technique is applicable to any DNA amplification method generating pyrophosphate (PPi) as a by-product.

Colorimetric detection of alkaline phosphatase on paper microfluidic test strip based on the in-situ formation of gold nanoparticles

Affordable alkaline phosphatase enzyme detection methods are essential for diagnosing hepatic diseases. In this work, an in-situ formation of gold nanoparticles was utilized to develop a colorimetric method to detect alkaline phosphatase. Alkaline phosphatase dephosphorylates the substrate 2-phospho-L-ascorbic acid and produces ascorbic acid. Ascorbic acid, thus formed, is a good reducing agent that reduces Au3+ ions to gold nanoparticles. Alkaline phosphatase concentrations from 20 U/L to 400 U/L were spectrophotometrically detected using the surface plasmon resonance properties of the in-situ formed gold nanoparticles. The detection shows a sensitivity of 0.004 ± 0.0002 (a.u)/(U/L), a limit of detection of 2.8 mU/L, and a limit of quantification of 9.5 mU/L. A three-dimensional microfluidic paper test strip was fabricated to translate this detection method into a point-of-care testing device. The blue color formed on the paper was scanned, and the color intensities were analyzed using image processing. The three-dimensional microfluidic paper-based analytical devices could detect alkaline phosphatase concentration from 20 U/L to 400 U/L with an improved sensitivity of 0.0980 ± 0.0016 (a.u)/(U/L). The limit of detection and limit of quantification of the analysis on the paper strip was 0.748 U/L and 2.49 U/L, respectively.

Visual‐Detection of Cu2+ in DMSO aAqueous Solution Based on Benzimidazole Azo‐dye as a Colorimetric Chemosensor

AbstractIn this work, a novel colorimetric chemosensor (BIAD) containing azo chromophore, 1,5dihydroxynaphthalene, and benzimidazole was synthesized and characterized by using IR, 1H,13C NMR, and mass spectral data, and elemental analysis. The cation recognition studies (including fourteen metal cations) exhibited that the synthesized azo dye can act as a rapid, sensitive, and selective colorimetric chemosensor for detecting Cu2+ ions. The addition of Cu2+ ions to the BIAD solution, changed immediately the solution color from purple to blue‐green, which could be observed by the naked eye. Comparison of the UV/Visible spectra of BIAD and (BIAD+Cu2+) revealed a red shift from 543 nm to 616 nm, which confirms the formation of a complex between Cu2+ cations and BIAD molecules. The result of Job's plot indicated that the stoichiometry binding ratio of BIAD to Cu2+ is 1 : 1. The limit of detection (LOD) was found for BIAD toward Cu2+ ion to be 0.10 μM. Furthermore, the BIAD‐based test paper strips were successfully used for the rapid detection of Cu2+ ions (<1 sec) in the aqueous solution (H2O‐DMSO, 9 : 1).

Development of a simple and rapid dipstick paper-based test strip for colorimetric determination of nitrate and nitrite in water and foodstuffs

A rapid user-friendly paper-based test strip using zinc microparticles in conjugation with Griess reagent was developed for nitrite and nitrate detection. Test strips were fabricated using a simple and fast method of step-by-step immersion into reagents so that each strip contained a single detection pad for nitrite detection and another separate pad for nitrate detection. To reduce nitrate to nitrite, zinc microparticles suspended in ethanolic solution of polyvinylpyrrolidone (PVP) were uniformly immobilized on the paper strips that were previously impregnated in the Griess reagent and dried. The Griess reagent components were optimized to reach the highest color intensity. The optimized test strip was able to determine both nitrite and nitrate with respective detection limits of 0.43 and 9.43 mg/kg and a detection time of 60 s. The performance of the new test strips was evaluated for the simultaneous colorimetric detection of nitrite and nitrate in water and different food samples.

Sensing features, on-site detection and bio-imaging application of a tripodal tris(hydroxycoumarin) based probe towards Cu2+/His

A new tripodal tris(hydroxycoumarin) based Schiff base, HCTN was synthesized and characterized by FT-IR, 1H NMR, 13C NMR and ESI-HRMS. The probe, HCTN exhibits cyan emission in DMSO/HEPES buffer (9:1, v/v) which selectively detects Cu2+ ion via turn-off fluorescence. The quenching of the fluorescence was due to the binding of the probe, HCTN towards paramagnetic Cu2+ ion resulting in chelation enhanced quenching effect (CHEQ). From the spectroscopic results, the limit of detection of Cu2+ ion was obtained as very low as 0.40 × 10−9 M. The complexation of the metal ion, Cu2+ towards the probe HCTN was confirmed by the ESI-HRMS and Job’s plot analysis which supports 1:1 binding stochiometric ratio. In order to validate the affinity of Cu2+ ion towards histidine, the HCTN+Cu2+ system was utilized for the detection of histidine via turn-on mode by the metal displacement approach. The detection limit of His was found to be 7.31 × 10−10 M. In addition to the above, the probe was utilized for various detection applications such as paper strips, cotton swabs, logic gates and thin film applications. The probe, HCTN extends its application to the confocal bioimaging to sense the Cu2+ and Histidine intracellularly.

A Versatile pH-Dependent Fluorometric, Colorimetric, and Electrochemical Sensor for H2S Monitoring in Water.

Hydrogen sulfide (H2S) is a colorless, foul smelling, toxic substance that can be found in water bodies and waste waters, especially in occupational susceptible environments, and can lead to harmful effects in humans at higher concentrations. An H2S monitoring probe NNAP is synthesized, which displays pH-dependent electrochemical, colorimetric, and fluorescence responses. NNAP functions as a fluorometric sensor at pH 7.4, with a limit of detection (LOD) of 0.70 mM, and as a colorimetric sensor at pH 12, where visible color changes are discernible to the naked eye, with an LOD of 4.28 mM. Additionally, it demonstrates utility in electrochemical sensing at pH 2, with a LOD of 2.5 mM. Furthermore, NNAP-coated paper strips have been successfully utilized for real-time H2S monitoring applications.

Investigation of bone remodeling in gingival crevicular fluid in patients treated with rapid maxillary expansion during pubertal period

Purpose: We aimed to evaluate bone remodeling following 3-month and 6-month retention periods of rapid maxillary expansion (RME) in gingival crevicular fluid (GCF). Materials and Methods: 23 pubertal participants (15 girls- 8 boys, 12-15 years) with maxillary transversal deficiency were enrolled in the study. Following banded-type RME appliance was introduced into the mouth, RME protocol was initiated by turning the Hyrax screw twice daily (morning/evening) with ¼ activation. GCF samples were taken from right maxillary first molars at four different time points (T0: before the appliance was deployed, T1: following active phase, T2: at the end of the 3-month retention period, T3: at the end of the 6-month retention period) using paper strips. Probing depth, gingival index, plaque index, and bleeding percentage at probing were recorded. BALP, OPG, RANKL, and TNF-α levels were measured in GCF samples using ELISA kits. Results: Our study revealed that GCF's BALP and OPG levels remained unchanged over time in tension and pressure regions, and there were no statistically significant differences among regions at each time point (p>0.05). RANKL level was statistically significantly increased in the buccal region (the pressure region) at time T1 (p=0.042). The palatinal region's TNF-α level was statistically significantly higher than the buccal region at T0, T2, and T3 time points (p=0.005, p=0.042, and p=0.006, respectively). Our study showed no correlation between 3-month and 6-month retention periods and biomarkers indicating RME's bone metabolic activities. Conclusions: Further studies with different retention periods and larger sample sizes are suggested.

Trimetallic FeCoNi Metal-Organic Framework with Enhanced Peroxidase-like Activity for the Construction of a Colorimetric Sensor for Rapid Detection of Thiophenol in Water Samples.

In recent years, nanozymes have attracted particular interest and attention as catalysts because of their high catalytic efficiency and stability compared with natural enzymes, whereas how to use simple methods to further improve the catalytic activity of nanozymes is still challenging. In this work, we report a trimetallic metal-organic framework (MOF) based on Fe, Co and Ni, which was prepared by replacing partial original Fe nodes of the Fe-MOF with Co and Ni nodes. The obtained FeCoNi-MOF shows both oxidase-like activity and peroxidase-like activity. FeCoNi-MOF can not only oxidize the chromogenic substrate 3,3,5,5-tetramethylbenzidine (TMB) to its blue oxidation product oxTMB directly, but also catalyze the activation of H2O2 to oxidize the TMB. Compared with corresponding monometallic/bimetallic MOFs, the FeCoNi-MOF with equimolar metals hereby prepared exhibited higher peroxidase-like activity, faster colorimetric reaction speed (1.26-2.57 folds), shorter reaction time (20 min) and stronger affinity with TMB (2.50-5.89 folds) and H2O2 (1.73-3.94 folds), owing to the splendid synergistic electron transfer effect between Fe, Co and Ni. Considering its outstanding advantages, a promising FeCoNi-MOF-based sensing platform has been designated for the colorimetric detection of the biomarker H2O2 and environmental pollutant TP, and lower limits of detection (LODs) (1.75 μM for H2O2 and 0.045 μM for TP) and wider linear ranges (6-800 μM for H2O2 and 0.5-80 μM for TP) were obtained. In addition, the newly constructed colorimetric platform for TP has been applied successfully for the determination of TP in real water samples with average recoveries ranging from 94.6% to 112.1%. Finally, the colorimetric sensing platform based on FeCoNi-MOF is converted to a cost-effective paper strip sensor, which renders the detection of TP more rapid and convenient.